AZITHROMYCIN ANTIMICROBIAL SUSCEPTIBILITY TEST DISC

{0}------------------------------------------------ Food and Drug Administration 2098 Gaither Road Rockville MD 20850 Andy Hollingsworth Quality Systems Manager Oxoid Limited ... ......... Wade Road Basingstoke Hants RG24 8PW England JUL - 3 1997 Re: K971635 Trade Name: Azithromycin Antimicrobial Susceptibility Test Disc Regulatory Class: II Product Code: JTN Dated: June 10, 1997 Received: June 12, 1997 Dear Mr. Hollingsworth: We have reviewed your Section 510(k) notification of intent to market the device referenced above and we have determined the device is substantially equivalent (for the indications for use stated in the enclosure) to devices marketed in interstate commerce prior to May 28, 1976, the enactment date of the Medical Device Amendments or to devices that have been reclassified in accordance with the provisions of the Federal Food, Drug, and Cosmetic Act (Act). You may, therefore, market the device, subject to the general controls provisions of the Act. The general controls provisions of the Act include requirements for annual registration, listing of devices, good manufacturing practice, labeling, and prohibitions against misbranding and adulteration. If your device is classified (see above) into either class II (Special Controls) or class III (Premarket Approval), it may be subject to such additional controls. Existing major regulations affecting your device can be found in the Code of Federal Regulations. Title 21, Parts 800 to 895. A substantially equivalent determination assumes compliance with the Good Manufacturing Practice for Medical Devices: General (GMP) regulation (21 CFR Part 820) and that, through periodic GMP inspections, the Food and Drug Administration (FDA) will verify such assumptions. Failure to comply with the GMP regulation may result in regulatory action. In addition, FDA may publish further announcements concerning your device in the Federal Register. Please note: this response to your premarket notification submission does not affect any obligation you might have under sections 531 through 542 of the Act for devices under the Electronic Product Radiation Control provisions, or other Federal Laws or Regulations. Image /page/0/Picture/10 description: The image shows the seal of the U.S. Department of Health & Human Services. The seal features a stylized caduceus-like symbol with three wavy lines emanating from a central point, resembling a bird in flight. The text "DEPARTMENT OF HEALTH & HUMAN SERVICES - USA" is arranged in a circular pattern around the symbol. {1}------------------------------------------------ Under the Clinical Laboratory Improvement Amendments of 1988 (CLIA-88), this device may require a CLIA complexity categorization. To determine if it does, you should contact the Centers for Disease Control and Prevention (CDC) at (770)488-7655. ---------- This letter will allow you to begin marketing your device as described in your 510(k) premarket notification. The FDA finding of substantial equivalence of your device to a legally marketed predicate device results in a classification for your device and thus, permits your device to proceed to the market. If you desire specific advice for your device on our labeling regulation (21 CFR Part 801 and additionally 809.10 for in vitro diagnostic devices), please contact the Office of Compliance at (301) 594-4588. Additionally, for questions on the promotion and advertising of your device, please contact the Office of Compliance at (301) 594-4639. Also, please note the regulation entitled, "Misbranding by reference to premarket notification" (21 CFR 807.97). Other general information on your responsibilities under the Act may be obtained from the Division of Small Manufacturers Assistance at its toll free number (800) 638-2041 or at (301) 443-6597 or at its internet address "http://www.fda.gov/cdrh/dsmamain.html" Sincerely yours. Steven Sutman Steven I. Gutman, M.D., M.B.A. Director Division of Clinical Laboratory Devices Office of Device Evaluation Center for Devices and Radiological Health Enclosure {2}------------------------------------------------ ## 510(K) Submission for Oxoid Antimicrobial Susceptibility Test Disc ## AZITHROMYCIN ## OXOID LTD K971635 510(K) Number : Oxoid Azithromycin Susceptibility Test Disc Device Name : ## Indication for Use : Antimicrobial Susceptibility Test Discs are indicated for the semi-quantitative susceptibility testing by agar diffusion test procedure of rapidly growing micro-organisms. These include : Staphylococcus spp., modified by procedures, Haemophilus influenzae, Streptococcus pneumoniae. The technical product insert details the Quality Control organisms to be use with this disc. Arlin Perika (Division Sign-Off) Division of Clinical Laboratory Devices 510(k) Number_ \/ for prescription use Image /page/2/Picture/11 description: The image shows a black and white abstract shape. The shape is mostly black with some white speckles. The shape is round and irregular.